Canonical Allele Identifier: CA350386742

Gene: SATB2

Linked Data

• MyVariant Identifiers: chr2:g.200298123T>G (hg19) ; chr2:g.199433400T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.199433400T>G , CM000664.2:g.199433400T>G	GRCh38
NC_000002.11:g.200298123T>G , CM000664.1:g.200298123T>G	GRCh37
NC_000002.10:g.200006368T>G	NCBI36
NG_016976.1:g.42867A>C
NG_016976.2:g.42867A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000428695.6:c.284A>C	ENSP00000388581.1:p.Gln95Pro
ENST00000700191.1:c.284A>C	ENSP00000514853.1:p.Gln95Pro
ENST00000700193.1:c.284A>C	ENSP00000514854.1:p.Gln95Pro
ENST00000700194.1:n.542A>C
ENST00000700208.1:c.284A>C	ENSP00000514860.1:p.Gln95Pro
ENST00000417098.6:c.284A>C MANE Select	ENSP00000401112.1:p.Gln95Pro
ENST00000260926.9:c.284A>C	ENSP00000260926.5:p.Gln95Pro
ENST00000417098.5:c.284A>C	ENSP00000401112.1:p.Gln95Pro
ENST00000428695.5:c.284A>C	ENSP00000388581.1:p.Gln95Pro
ENST00000440919.1:c.284A>C	ENSP00000415610.1:p.Gln95Pro
ENST00000443023.5:c.169+22469A>C	ENSP00000388764.1:n.169+22469A>C
ENST00000457245.5:c.284A>C	ENSP00000405420.1:p.Gln95Pro
ENST00000614512.4:c.284A>C	ENSP00000483287.1:p.Gln95Pro
NM_001172509.1:c.284A>C	NP_001165980.1:p.Gln95Pro
NM_001172517.1:c.284A>C	NP_001165988.1:p.Gln95Pro
NM_015265.3:c.284A>C	NP_056080.1:p.Gln95Pro
XM_005246396.1:c.110A>C	XP_005246453.1:p.Gln37Pro
XM_006712372.1:c.284A>C	XP_006712435.1:p.Gln95Pro
XM_011510840.1:c.284A>C	XP_011509142.1:p.Gln95Pro
NR_134967.1:n.1101A>C
XM_005246396.3:c.110A>C	XP_005246453.1:p.Gln37Pro
XM_011510840.3:c.284A>C	XP_011509142.1:p.Gln95Pro
XM_017003656.1:c.110A>C	XP_016859145.1:p.Gln37Pro
XM_024452767.1:c.-350A>C	XP_024308535.1:n.-350A>C
NM_001172509.2:c.284A>C MANE Select	NP_001165980.1:p.Gln95Pro
NM_015265.4:c.284A>C	NP_056080.1:p.Gln95Pro
NR_134967.2:n.944A>C